Aysylu F Murtazina (Aisylu Murtazina, Aysylu Murtazina, A F Murtazina)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 13

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Top Venues

International journal of molecular sciences

Molecular biology reports

This page only lists publications with an associated author ORCID identifier.

Publications

Sofya A Ionova, Aysylu F Murtazina, Andrey A Marakhonov, Olga A Shchagina, Nina V Ryadninskaya, Inna S Tebieva, Vitaly V Kadyshev, Artem O Borovikov, Evgeny K Ginter, Sergey I Kutsev, Rena A Zinchenko
The Study of the Inheritance Mechanisms of Myotonic Dystrophy Type 1 (DM1) in Families from the Republic of North Ossetia-Alania. International journal of molecular sciences 25 (17) (2024)
Aysylu F Murtazina, Artem O Borovikov, Anna Kuchina, Olga Ovsova, Maria Bulakh, Alena Chukhrova, Svetlana Braslavskaya, Oxana P Ryzhkova, Nikolay Skryabin, Sergey Kutsev, Elena Dadali
Expanding the Phenotype of Hereditary Congenital Facial Paresis Type 3. International journal of molecular sciences 25 (1) (2023)
Olga A Shchagina, Mariya Orlova, Aysylu F Murtazina, Alexandra Yu Filatova, Mikhail Yurevich Skoblov, Elena Dadali
Evaluation of Pathogenicity and Causativity of Variants in the MPZ and SH3TC2 Genes in a Family Case of Hereditary Peripheral Neuropathy. International journal of molecular sciences 24 (12) (2023)
Polina Chausova, Aysylu F Murtazina, Anna Stepanova, Artem O Borovikov, Valeriia A Kovalskaia, Nina Ryadninskaya, Alena Chukhrova, Oxana P Ryzhkova, Aleksander Poliakov
X-Linked Myotubular Myopathy in a Female Patient with a Pathogenic Variant in the MTM1 Gene. International journal of molecular sciences 24 (9) (2023)
Polina Chausova, Aysylu F Murtazina, Anna Stepanova, Artem O Borovikov, Valeriia A Kovalskaia, Nina Ryadninskaya, Alena Chukhrova, Oxana P Ryzhkova, Aleksander Poliakov
X-Linked Myotubular Myopathy in a Female Patient with a Pathogenic Variant in the MTM1 Gene. International journal of molecular sciences 24 (9) (2023)
Polina Chausova, Aysylu F Murtazina, Anna Stepanova, Artem O Borovikov, Valeriia A Kovalskaia, Nina Ryadninskaya, Alena Chukhrova, Oxana P Ryzhkova, Aleksander Poliakov
X-Linked Myotubular Myopathy in a Female Patient with a Pathogenic Variant in the MTM1 Gene. International journal of molecular sciences 24 (9) (2023)
Olga A Shchagina, Mariya Orlova, Aysylu F Murtazina, Alexandra Yu Filatova, Mikhail Yurevich Skoblov, Elena Dadali
Evaluation of Pathogenicity and Causativity of Variants in the MPZ and SH3TC2 Genes in a Family Case of Hereditary Peripheral Neuropathy. International journal of molecular sciences 24 (12) (2023)
Aysylu F Murtazina, Artem O Borovikov, Anna Kuchina, Olga Ovsova, Maria Bulakh, Alena Chukhrova, Svetlana Braslavskaya, Oxana P Ryzhkova, Nikolay Skryabin, Sergey Kutsev, Elena Dadali
Expanding the Phenotype of Hereditary Congenital Facial Paresis Type 3. International journal of molecular sciences 25 (1) (2023)
Aysylu F Murtazina, Artem O Borovikov, Anna Kuchina, Olga Ovsova, Maria Bulakh, Alena Chukhrova, Svetlana Braslavskaya, Oxana P Ryzhkova, Nikolay Skryabin, Sergey Kutsev, Elena Dadali
Expanding the Phenotype of Hereditary Congenital Facial Paresis Type 3. International journal of molecular sciences 25 (1) (2023)
Olga A Shchagina, Mariya Orlova, Aysylu F Murtazina, Alexandra Yu Filatova, Mikhail Yurevich Skoblov, Elena Dadali
Evaluation of Pathogenicity and Causativity of Variants in the MPZ and SH3TC2 Genes in a Family Case of Hereditary Peripheral Neuropathy. International journal of molecular sciences 24 (12) (2023)
Aysylu F Murtazina, Nina Demina, Polina Chausova, Olga A Shchagina, Artem O Borovikov, Elena Dadali
The First Russian Patient with Native American Myopathy. Genes 13 (2) (2022)
Aysylu F Murtazina, Sergey Nikitin, Galina Rudenskaya, Inna Sharkova, Artem O Borovikov, Peter A Sparber, Olga A Shchagina, Alena Chukhrova, Oxana P Ryzhkova, Olga Mironovich, Anna A Orlova, Vasilisa Udalova, Ilya Kanivets, Sergey Korostelev, Alexander Polyakov, Elena Dadali, Sergey Kutsev
Genetic and Clinical Spectrum of GNE Myopathy in Russia. Genes 13 (11) (2022)
Olga A Shchagina, Tatiana B Cherevatova, Aysylu F Murtazina, G E Rudenskaya, S S Nikitin, E L Dadali, Alexander V Polyakov
HINT1 gene pathogenic variants: the most common cause of recessive hereditary motor and sensory neuropathies in Russian patients. Molecular biology reports 47 (2) (2019)